TY - JOUR
T1 - Checkpoint modulation in melanoma
T2 - An update on ipilimumab and future directions
AU - Page, David B.
AU - Postow, Michael A.
AU - Callahan, Margaret K.
AU - Wolchok, Jedd D.
N1 - Funding Information:
Jedd D. Wolchok has been a consultant for Bristol-Myers Squibb and Merck, has received grants from Bristol-Myers Squibb, Merck, and AstraZeneca, and has received travel accommodation from Bristol-Myers Squibb. David B. Page declares no conflict of interest.
Funding Information:
Conflict of Interest Margaret K. Callahan has received a research grant from Bristol-Myers Squibb.
PY - 2013/10
Y1 - 2013/10
N2 - Ipilimumab, an anti-cytotoxic T-lymphocyte antigen 4 antibody, was the first therapy demonstrated to improve overall survival in melanoma. Since ipilimumab's approval by the FDA in 2011, a wealth of data has amassed, helping clinicians to optimize its use. We have learned how to mitigate the adverse effects of ipilimumab, identified its effects in melanoma subpopulations such as those with brain metastases, uveal melanoma, and mucosal melanoma, discovered potential biomarkers of activity, and investigated its use in combination with other therapeutic modalities. These discoveries have paved the way for rapid development of second-generation immunomodulatory antibodies such as inhibitors of the programmed cell death 1 receptor axis. These new agents hold promise as monotherapy, but perhaps the greatest allure lies in the possibility of combining these agents in synergistic multidrug regimens.
AB - Ipilimumab, an anti-cytotoxic T-lymphocyte antigen 4 antibody, was the first therapy demonstrated to improve overall survival in melanoma. Since ipilimumab's approval by the FDA in 2011, a wealth of data has amassed, helping clinicians to optimize its use. We have learned how to mitigate the adverse effects of ipilimumab, identified its effects in melanoma subpopulations such as those with brain metastases, uveal melanoma, and mucosal melanoma, discovered potential biomarkers of activity, and investigated its use in combination with other therapeutic modalities. These discoveries have paved the way for rapid development of second-generation immunomodulatory antibodies such as inhibitors of the programmed cell death 1 receptor axis. These new agents hold promise as monotherapy, but perhaps the greatest allure lies in the possibility of combining these agents in synergistic multidrug regimens.
KW - Anti-programmed cell death 1
KW - Checkpoint
KW - Immunotherapy
KW - Ipilimumab
KW - Melanoma
UR - https://www.scopus.com/pages/publications/84884586706
U2 - 10.1007/s11912-013-0337-1
DO - 10.1007/s11912-013-0337-1
M3 - Article
C2 - 23933888
AN - SCOPUS:84884586706
SN - 1523-3790
VL - 15
SP - 500
EP - 508
JO - Current Oncology Reports
JF - Current Oncology Reports
IS - 5
ER -